ClearanceBrief
510(k) K943199 ยท IYE Accelerator, Linear, Medical

MOTORIZED DEPTH DOSE APPARATUS

ApplicantMedtec, Inc., Orange City IA, US
DecisionSubstantially Equivalent, Dec 7, 1994
ReceivedJul 5, 1994
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K943199

No recall in the FDA data names this 510(k).

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.